Technician II, Quality Control Lab

Overview COMPANY OVERVIEW: At Alcon, we are inspired by the meaningful work we do to help people see brilliantly. As the global leader in eye care, we boldly innovate, champion progress, and act with speed. We recognize and celebrate the contributions of our people, offering career opportunities that empower growth and fulfillment. Together, we go above and beyond to make a lasting impact on the lives of our patients and customers. We cultivate an inclusive culture and invite diverse, talented individuals to join us in shaping the future of eye care. At Alcon, we are committed to fostering a work environment where our employees can grow, innovate, and excel. Here’s how you can thrive in your role with us: career growth & development, collaborative culture, impactful work, recognition & rewards, global exposure, and work-life balance & well-being. Role Summary As a Technician II, Quality Control Lab – Chemistry , you will play a key role in supporting manufacturing operations by performing chemical analyses, maintaining laboratory equipment, and ensuring compliance with regulatory standards. This is an excellent opportunity for individuals passionate about laboratory work and quality assurance in a dynamic, regulated environment. Responsibilities Perform testing and/or inspection on raw material, in-process material, finished products and monitoring activities. Review/Approve testing documentation and test records. Maintain integrity, accuracy and completeness of QC data and records. Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements. Timely completion of all compliance activities without overdue, including but not limited to NCI, OOS, CAPA, Effectiveness Check, CR, training, periodic review. Timely report non-conformance or out-of-specification events. Lead or assist in root cause analyses for product defects and quality lapses, and take effective actions to prevent recurrence. Drive and promote the continuous improvement culture. Challenge current processes, identify improvements and drive the effort to implement lab system/process while maintaining compliance and reducing human Intervention. Review and assess external standard and/or regulatory requirements pertaining to quality control activities and implement necessary changes to ensure compliance Perform basic equipment troubleshooting. Qualifications Diploma (with at least 3 years) or Degree (with at least 1 year) in Chemistry, Biotechnology, or a related scientific discipline. Prior experience in a GMP-regulated laboratory environment is preferred. Familiarity with analytical techniques such as HPLC, UV-Vis etc. Strong attention to detail, documentation skills, and commitment to quality. Ability to work effectively in a team-oriented and fast-paced environment. Willingness to work rotational shift schedule across 3x shifts. How you can thrive at Alcon Career Growth & Development – Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey. Collaborative Culture – Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork. Impactful Work – Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide. Recognition & Rewards – Your contributions are valued and recognized through competitive compensation, performance incentives and career progression opportunities. Global Exposure – Join a world-class organization with opportunities to collaborate across international teams and gain global industry insights. Work-Life Balance & Well-Being – Enjoy employee wellness programs, flexible work arrangements and initiatives that support your well-being. Additional Details Seniority level: Entry level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industries: Medical Equipment Manufacturing ATTENTION: If you are currently an active employee/contingent worker at Alcon, please apply on the Internal Career site. #J-18808-Ljbffr